Question | Answer |
How are Esters Formed? | Condensation reaction between a carboxyllic acid and an alcohol |
How can you tell is an Ester has been made? | An oily layer will have formed and an aroma let off |
How are esters prepared in the lab? | In a water bath and using a condenser |
Why is the ester reaction heated using a water bath as opposed to an open flame? | The alcohol used is flammable, this would be dangerous with an open flame |
What is produced upon the hydrolysis of an ester? | a carboxyllic acid and an alcohol |
What are esters used for? | fruit flavourings non-polar industrial solvents |
What are the three types of fats and oils? Give an example of each. | Marine - blubber Animal - goose fat Vegetable - Olive oil |
Why is there a difference in the melting point of fats and oils? | Differing number of C=C bonds |
Which have a higher melting point, oils or fats? | Fats, no C=C bonds |
Fat as an energy source | Slow release energy releases more energy per gram than carbohydrates extra energy is stored as fat |
Structure of fat | One mol of glycerol to 3 mols of fatty acid |
How are all fats and oils similar? | They are all esters of the same alcohol |
What is this? | Glycerol |
What is used to catalyse the hardening of oils? | Nickel |
What is the hardening of oils? | hydrogenating to reduce the number of C=C bonds, thus reducing the melting point and degree of saturation |
What is a saturated carboxyllic acid? | Carboxyllic acid with no C=C bonds |
What is an unsaturated Carboxyllic acid | Carboxyllic acid with C=C bonds |
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